Haematological Malignancy Flashcards

1
Q

Haematological Malignancies Epidemiology

A

10% of all human cancers
Occur in all age groups, including children

Adult males are more commonly affected than females.

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2
Q

Common cancer in children

A

Acute Lymphoblastic Leukaemia

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3
Q

Age of Hodgkin Lymphoma

A

Peak incidence between 18-35

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4
Q

Median age for MDS

A

73-74

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5
Q

Characteristics of Multipotential haemopoietic stem cell

A

Cant identify them down the microscope
Can identify them with immunophenotyping
Small population of the bone marrow.
They are pluripotent, and undergo self-renewal

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6
Q

Myeloid Malignancies

A

Red cells, platelets, granulocytes and monocytes

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7
Q

Lymphoid malignancies

A

B-cell to T-cell

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8
Q

AML Mutation

A

Occurs at the hematopoetic cells or the myeloid progenitor cells. Proliferation but without differentiation resulting in the accumulation of useless progenitor cells.

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9
Q

ALL Mutation

A

Occurs at the hematopoetic cells or the lymphoid progenitor cells. Proliferation but without differentiation resulting in the accumulation of useless progenitor cells.

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10
Q

Myeloproliferative Disorders

A

Overproduction but with differentiation resulting in myeloproliferative disorders.

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11
Q

Mature Lymphoid malignancies

A

Occur as the cells pass through the germinal centre of the secondary lymphoid organs.

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12
Q

Leukaemia vs Lymphoma

A

If disease occurs in the bone marrow its called leukaemia

If disease occurs in the lymphoid tissue and solid organs then it is termed lymphoma.

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13
Q

Acute Leukaemias

A

Acute lymphoblastic leukaemia (ALL)

Acute Myeloid Leukaemia (AML)

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14
Q

Chronic Leukaemias

A

Chronic myeloid leukaemia (CML)

Chronic lymphocytic leukaemia (CLL)

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15
Q

Malignant Lymphoma

A
Non-Hodgkin lymphoma (NHL)
Hodgkin lymphoma (HL)
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16
Q

Multiple myeloma

A

Malignany of plasma cells

17
Q

Acute leukaemia process

A

Leukaemic cells do not differentiate
Bone marrow failure
Rapidly fatal if untreated
Potentially curable

18
Q

Chronic leukaemia process

A

Leukaemic cells retain ability to differentiate
Proliferation without bone marrow failure
Survival for a few years
Not presently curable without BMT

19
Q

Clinical features of acute leukaemia (bone marrow failure)

A

Anaemia

  • Thrombocytopenic bleeding (Purpura and mucosal membrane bleeding)
  • Infection because of neutropenia (predominantly bacterial and fungal)
20
Q

Structure of the Lymph Node

A

Different lymphocyte populations reside in different areas of the node – B cells in the follicles. T cells in the paracortex and plasma cells in the medulla. Within the B-cell areas different populations – Cells undergoing expansion and selection in the GCs, naive cells in the mantle zone

21
Q

B-cell maturation

A

B-cell must display appropriate IG to the antigen to survive

22
Q

Lymphoma Presentations

A

Nodal disease – Lymphadenopathy
> 90% HL present with nodal disease
~ 60% NHL present with purely nodal disease

Extranodal disease:
~ 40% NHL present with an extranodal component

Systemic symptoms: fever, drenching sweats, loss of weight, pruitis, fatigue

23
Q

Localised and painful lymphadenopathy

A

Bacterial infection in draining site

24
Q

Localised and painless lymphadenopathy

A

Rare infections, catch scratch fever, TB
Metastatic carcinoma from draining site- hard
Lymphoma-rubbery
Reactive, no cause identified

25
Q

Generalised and painful lymphadenopathy

A

Viral infections, EBV, CMV, hepatitis, HIV

26
Q

Generalised and painless lymphadenopathy

A
Lymphoma
Leukaemia
Connective tissue diseases, sarcoidosis
Reactive, no cause identified
Drugs
27
Q

Multiple Myeloma Clinical features

A
Bone pain and lytic lesions
Hyper viscosity syndrome
Bleeding tendency
Amyloidosis
Renal failure
Recurrent infections
Anaemia